NEKVNRO SNOW BLEACH CREAM- snow bleach cream liquid

Nekvnro Snow Bleach Cream by

Drug Labeling and Warnings

Nekvnro Snow Bleach Cream by is a Otc medication manufactured, distributed, or labeled by Guoyu Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

NIACINAMIDE 15%

Purpose

Anti-hyperpigmentation

Use

Used to whiten or lighten skin pigmentation.

Warnings

For external use only.

Do not use

if irritation or allergic reactions develop.
on damaged or broken skin. on individuals aged 12 and under.

When Using

section When using this productavoid contact with eyes.
Please test this cream on a small patch of your the inside of the arm if it is your first time using this cream.
Stop use section If pregnant or breast-feeding, ask a health professional before use.

Stop Use

Discontinue use if signs of irritation or rash occur.

Ask Doctor

Discontinue use if signs of irritation or rash occur.

Keep Oot Of Reach Of Children

Please keep out of reach of children.

Directions

Place enough product on hands to cover all surfaces.
Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

EDITStore between 15-30C (59-86F) Avoid freezingand excessive heat above 40C (104F)

Inactive ingredients

ASCORBIC ACID，WATER，CHAMOMILE，CENTELLA ASIATICA，ALLANTOIN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO SNOW BLEACH CREAM 
snow bleach cream liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
WATER (UNII: 059QF0KO0R)
CHAMOMILE (UNII: FGL3685T2X)
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-005-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/31/2024
2	NDC: 84844-005-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/31/2024

Labeler - Guoyu Trading Co., Ltd. (963348600)

Establishment
Name	Address	ID/FEI	Business Operations
Guoyu Trading Co., Ltd.		963348600	manufacture(84844-005)